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Solutions for Chapter 6.5c: SOLUTIONS OF SOLIDS IN LIQUIDS

Elementary Principles of Chemical Processes | 4th Edition | ISBN: 9780470616291 | Authors: Richard M. Felder Ronald W. Rousseau, Lisa G. Bullard

Full solutions for Elementary Principles of Chemical Processes | 4th Edition

ISBN: 9780470616291

Elementary Principles of Chemical Processes | 4th Edition | ISBN: 9780470616291 | Authors: Richard M. Felder Ronald W. Rousseau, Lisa G. Bullard

Solutions for Chapter 6.5c: SOLUTIONS OF SOLIDS IN LIQUIDS

Chapter 6.5c: SOLUTIONS OF SOLIDS IN LIQUIDS includes 5 full step-by-step solutions. Since 5 problems in chapter 6.5c: SOLUTIONS OF SOLIDS IN LIQUIDS have been answered, more than 41693 students have viewed full step-by-step solutions from this chapter. This textbook survival guide was created for the textbook: Elementary Principles of Chemical Processes, edition: 4. Elementary Principles of Chemical Processes was written by and is associated to the ISBN: 9780470616291. This expansive textbook survival guide covers the following chapters and their solutions.

Key Chemistry Terms and definitions covered in this textbook
  • amines.

    Organic bases that have the functional group —NR2, where R may be H, an alkyl group, or an aromatic group. (24.4)

  • antibonding MO

    A high-energy molecular orbital resulting from the destructive interference between atomic orbitals.

  • Aromatic compound

    A term used initially to classify benzene and its derivatives. More accurately, it is used to classify any compound that meets the Hückel criteria for aromaticity (Section 21.2A).

  • Azeotrope

    A liquid mixture of constant composition with a boiling point that is different from that of any of its components.

  • beta (b) rays.

    Electrons. (2.2)

  • bonding atomic radius

    The radius of an atom as defined by the distances separating it from other atoms to which it is chemically bonded. (Section 7.3)

  • Carbenoid

    A compound that delivers the elements of a carbene without actually producing a free carbene.

  • conservation of orbital symmetry

    During a reaction, the requirement that the phases of the frontier MOs must be aligned.

  • effective nuclear charge

    The net positive charge experienced by an electron in a many-electron atom; this charge is not the full nuclear charge because there is some shielding of the nucleus by the other electrons in the atom. (Section 7.2)

  • heat of fusion

    The enthalpy change, ?H, for melting a solid. (Section 11.4)

  • Nitrile

    A compound containing a !C#N (cyano) group bonded to a carbon atom.

  • overall reaction order

    The sum of the reaction orders of all the reactants appearing in the rate expression when the rate can be expressed as rate = k3A4a 3B4b... . (Section 14.3)

  • oxaphosphetane

    An intermediate that is believed to be formed during Wittig reactions.

  • phenoxide

    The conjugate base of phenol or a substituted phenol.

  • physical changes

    Changes (such as a phase change) that occur with no change in chemical composition. (Section 1.3)

  • radical

    A chemical entity with an unpaired electron.

  • Retrosynthesis

    A process of reasoning backwards from a target molecule to a suitable set of starting materials.

  • stereoisomers

    Compounds that have the same constitution but differ in the 3D arrangement of atoms.

  • Tesla (T)

    The SI unit for magnetic fi eld strength.

  • twist boat

    A conformation of cyclohexane that is lower in energy than a boat conformation but higher in energy than a chair conformation.

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